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114235

Sigma-Aldrich

1,3,5-Triallyl-1,3,5-triazine-2,4,6(1H,3H,5H)-trione

98%

Synonym(s):

1,3,5-Tri-2-propen-1-yl-1,3,5-triazine-2,4,6(1H ,3H ,5H )-trione, 1,3,5-Triallyl-1,3,5-triazinane-2,4,6-trione, 1,3,5-Triallylisocyanurate, 1,3,5-Triallylisocyanuric acid, 1,3,5-Tris-2′-propenylisocyanuric acid, Triallyl isocyanurate

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About This Item

Empirical Formula (Hill Notation):
C12H15N3O3
CAS Number:
1025-15-6
Molecular Weight:
249.27
Beilstein:
225482
EC Number:
213-834-7
MDL number:
MFCD00006554
UNSPSC Code:
12162002
PubChem Substance ID:
24847161
NACRES:
NA.23

Quality Level

200

Assay

98%

contains

500 ppm tert-butylhydroquinone as inhibitor

refractive index

n20/D 1.513 (lit.)

bp

149-152 °C/4 mmHg (lit.)

density

1.159 g/mL at 25 °C (lit.)

SMILES string

C=CCN1C(=O)N(CC=C)C(=O)N(CC=C)C1=O

InChI

1S/C12H15N3O3/c1-4-7-13-10(16)14(8-5-2)12(18)15(9-6-3)11(13)17/h4-6H,1-3,7-9H2

InChI key

KOMNUTZXSVSERR-UHFFFAOYSA-N

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General description

1,3,5-Triallyl-1,3,5-triazine-2,4,6(1H,3H,5H)-trione, also known as triallyl isocyanurate (TAIC), is a versatile monomer widely employed in polymer synthesis as a crosslinking agent or co-monomer. It is commonly used as a key component in various applications, including rubber and plastic industries, coatings, adhesives, elastomers, and in the development of dental restorative materials.

Application

1,3,5-Triallyl-1,3,5-triazine-2,4,6(1H,3H,5H)-trione can be used as:
  • A crosslinking agent or additive in the synthesis of polylactic acid /flax composite materials to enhance their properties and performance under gamma irradiation.
  • A monomer in the synthesis of flexible ionogels with good mechanical properties via in situ thiol-ene photopolymerization with trimethylolpropane tris(3-mercaptopropionate). These ionogels further find applications in electrochemical capacitors.
  • A monomer in the fabrication of the shape memory polymer substrates.
The Progress in Development of Dental Restorative Materials

Pictograms

Exclamation markHealth hazard
GHS07,GHS08

Signal Word

Warning

Hazard Statements

H302 - H373

Hazard Classifications

Acute Tox. 4 Oral - STOT RE 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

319.1 °F - closed cup

Flash Point(C)

159.5 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Chuanglong He et al.
Journal of biomedical materials research. Part A, 99(4), 655-665 (2011-09-29)
The radiation crosslinked poly(L-lactide) (PLLA) electrospun nanofibers have been developed with improved thermal stability and mechanical properties. Trially isocyanurate (TAIC) were added into PLLA solution at different weight ratios (1, 3, and 5%) and electrospun into nanofibrous mats, the mats
Qingbing Zeng et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 789(2), 265-272 (2003-05-14)
Biocompatible affinity adsorbents prepared from macroporous glycidyl methacrylate-triallyl isocyanurate copolymer (GT) has been used for removing circulating immune complexes (CICs). In this work, adsorption of circulating immune complexes on GT-based affinity adsorbents has been studied by using batch and hemoperfusion
Wonsung Choi et al.
Scientific reports, 7(1), 12037-12037 (2017-09-22)
Lithium-metal-based batteries, owing to the extremely high specific energy, have been attracting intense interests as post-Li-ion batteries. However, their main drawback is that consumption/de-activation of lithium metal can be accelerated when O
Zhiquan Li et al.
Photochemistry and photobiology, 95(5), 1219-1229 (2019-03-19)
Designing digital light processing (DLP) 3D printable photosensitive resins with antibacterial properties is especially vital because of their potential applications in various biomedical fields. In this contribution, a thiol-ene-acrylate ternary system with reduced volume shrinkage and fast photopolymerization rate was
Cheng-Lan Lin et al.
Journal of chromatography. A, 1272, 65-72 (2012-12-25)
This study describes the ability of triallyl isocyanurate (TAIC)-co-methacrylate ester polymer monoliths as stationary phases for the separation of hydrophilic compounds (phenolic acids, amino acids and catecholamines) in capillary electrochromatography (CEC) and ultra high pressure liquid chromatography (UHPLC). Several TAIC-co-methacrylate
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Articles

The Progress in Development of Dental Restorative Materials

With dentists placing nearly 100 million dental fillings into patients′ teeth annually in the U.S. alone, polymeric composite restoratives account for a very large share of the biomaterials market.

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